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STRATA II Adjusment Kit - Indonesia BPOM Medical Device Registration

STRATA II Adjusment Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003125133. The device is manufactured by PMC, LLC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
STRATA II Adjusment Kit
Analysis ID: AKL 21003125133

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

PMC, LLC

Country of Origin

United States

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda

Registration Date

Aug 21, 2021

Expiry Date

Jan 13, 2026

Product Type

Therapeutic Neurology Equipment

Central nervous system fluid shunt and components.

Non Electromedic Non Sterile

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